Canonical Allele Identifier: CA425909251

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44126373G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899234G>A , CM000664.2:g.43899234G>A	GRCh38
NC_000002.11:g.44126373G>A , CM000664.1:g.44126373G>A	GRCh37
NC_000002.10:g.43979877G>A	NCBI36
NG_008247.1:g.101772C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.241C>T
ENST00000472420.6:n.889C>T
ENST00000483489.2:n.241C>T
ENST00000681993.1:n.1362C>T
ENST00000682303.1:c.*3596C>T	ENSP00000508325.1:n.*3596C>T
ENST00000682308.1:c.3810C>T	ENSP00000507056.1:p.Ala1270=
ENST00000682434.1:n.1361C>T
ENST00000682480.1:c.3828C>T	ENSP00000508344.1:p.Ala1276=
ENST00000682546.1:c.3807C>T	ENSP00000508188.1:p.Ala1269=
ENST00000682585.1:c.3810C>T	ENSP00000506885.1:p.Ala1270=
ENST00000682595.1:n.4394C>T
ENST00000682607.1:c.2228C>T
ENST00000682612.1:c.662C>T
ENST00000682779.1:c.3801C>T	ENSP00000507947.1:p.Ala1267=
ENST00000682885.1:c.3765C>T	ENSP00000508036.1:p.Ala1255=
ENST00000682933.1:n.3884C>T
ENST00000683002.1:c.662C>T
ENST00000683072.1:n.4394C>T
ENST00000683080.1:n.1429C>T
ENST00000683125.1:c.3918C>T	ENSP00000507939.1:p.Ala1306=
ENST00000683213.1:c.3813C>T	ENSP00000507751.1:p.Ala1271=
ENST00000683220.1:c.3840C>T	ENSP00000507151.1:p.Ala1280=
ENST00000683329.1:n.4613C>T
ENST00000683346.1:c.*3685C>T	ENSP00000507458.1:n.*3685C>T
ENST00000683409.1:n.2417C>T
ENST00000683459.1:n.4397C>T
ENST00000683528.1:c.738C>T
ENST00000683590.1:c.3558C>T	ENSP00000506820.1:p.Ala1186=
ENST00000683623.1:c.3717C>T	ENSP00000507702.1:p.Ala1239=
ENST00000683645.1:n.4361C>T
ENST00000683796.1:c.*3682C>T	ENSP00000508221.1:n.*3682C>T
ENST00000683802.1:n.6735C>T
ENST00000683833.1:c.3801C>T	ENSP00000506852.1:p.Ala1267=
ENST00000683994.1:c.3810C>T	ENSP00000507181.1:p.Ala1270=
ENST00000684290.1:c.*1346C>T	ENSP00000507243.1:n.*1346C>T
ENST00000684306.1:c.*3723C>T	ENSP00000508384.1:n.*3723C>T
ENST00000684341.1:n.3830C>T
ENST00000684383.1:c.*3448C>T	ENSP00000506863.1:n.*3448C>T
ENST00000684418.1:n.4991C>T
ENST00000684433.1:n.194C>T
ENST00000684454.1:n.3160C>T
ENST00000684619.1:c.*3682C>T	ENSP00000508088.1:n.*3682C>T
ENST00000684743.1:n.6555C>T
ENST00000260665.12:c.3810C>T MANE Select	ENSP00000260665.7:p.Ala1270=
ENST00000260665.11:c.3810C>T	ENSP00000260665.7:p.Ala1270=
ENST00000419884.5:c.51C>T	ENSP00000414207.1:p.Ala17=
ENST00000463456.5:n.2853C>T
ENST00000472420.5:n.207C>T
ENST00000483489.1:n.284C>T
NM_133259.3:c.3810C>T	NP_573566.2:p.Ala1270=
XM_006711915.2:c.3732C>T	XP_006711978.1:p.Ala1244=
XM_011532473.1:c.3810C>T	XP_011530775.1:p.Ala1270=
XM_011532474.1:c.3810C>T	XP_011530776.1:p.Ala1270=
XM_017003117.1:c.3732C>T	XP_016858606.1:p.Ala1244=
XR_002958896.1:n.3852C>T
NM_133259.4:c.3810C>T MANE Select	NP_573566.2:p.Ala1270=